Nghĩa của từ dystrophia bullosa bằng Tiếng Việt
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Đặt câu có từ "dystrophia bullosa"
1. Objective:Analysis characteristic and regularity of epidermolysis bullosa type eruption.
2. Conclusion:Incidence of epidermolysis bullosa type eruption ought to be observed...
3. Analysis characteristic and regularity of epidermolysis bullosa type eruption.
4. Recessive dystrophic epidermolysis bullosa with junctional blisters includes both the classical epidermolysis bullosa hereditaria letalis Herlitz (Herlitz-Pearson type) and a recently separated more benign adult type.
5. Although epidermolysis bullosa acquisita is thought to be an autoimmune disease, epidermolysis bullosa is a group of inherited diseases in which epithelial adhesion protein defects lead to epithelial fragility and Bullae …
6. The two genetic disorders of Connective tissue are epidermolysis bullosa (EB) and Marfan syndrome
7. Conclusions The causes and clinical features of drug-induced bullosa epidermolysis are extremely complicated.
8. "Ueber familiaeres Vorkommen von 'Retinitis punctata albescens' (verbunden mit 'Dystrophia marginalis cristallinea corneae'), Glitzern des Glaskoerpers und anderen degenerativen Augenveraenderungen".
9. Methods A retrospective study was performed on 31 patients with drug-induced bullosa epidermolysis.
10. Objective:To study molecule in basement membrane by electron microscopy and indirect immunofluorescence in patients with inherited epidermolysis bullosa.
11. The relationship between these results and the phenomenology of epidermolysis bullosa hereditaria in skin is discussed.
12. Objective To explore the causes, clinical features and appropriate therapies of drug-induced bullosa epidermolysis.
13. Learn more about the different types of Blistering diseases, such as, dermatitis herpetiformis, epidermolysis bullosa, and bullous pemphigoid.
14. Objective : To identify gene mutation in a family with Weber - Cockayne type epidermolysis bullosa simplex ( WC - EBS ).
15. In epidermolysis bullosa hereditaria (e.b.h.) simplex, the mode of formation of the bulla is particularly remarkable.
16. In particular, epidermolysis bullosa hereditaria, the collodion baby phenotype and harlequin ichthyosis represent serious clinical challenges with neonatal onset.
17. 7 patients with epidermolysis bullosa hereditaria as well as 3 relatives were examined upon their coagulation system.
18. Objective : To identify gene mutation in a family with Weber - Cockayne type epidermolysis bullosa simplex ( EBS - WC ).
19. Concha bullosa happens when one of the Conchae, or turbinates, inside your nose becomes filled with a pocket of air
20. With regard to the death rate, exfoliative dermatitis was the highest, next was epidermolysis bullosa and Stevens-Johnson syndrome was the lowest.
21. Our investigations show that there is no conclusive evidence for adrenocortical insufficiency in patients with dystrophia myotonica as judged by the results of the intravenous modification of the ACTH test.
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23. Pustular psoriasis of the palms and soles, epidermolysis bullosa hereditaria, hand-foot-mouth-disease, acrodermatitis enteropathica and scabies in children are possible differential diagnoses for vesicles on the palms and soles.
24. With vesicles, oozing or bullae: Pustular psoriasis of the palms and soles, epidermolysis bullosa hereditaria, hand-foot-mouth-disease, acrodermatitis enteropathica and scabies in children are possible differential diagnoses for vesicles on the palms and soles.
25. NYK, MTI unveil energy-saving adjustments to container vessel Of the 68 cases of concha bullosa, 31 cases (45.6%) were of extensive type (Figure 1), 21 cases (30.9%) were of Bulbous type (Figures 2, 3 and 4) and 16 cases (23.5%) were of lamellar type (Figure 5).